Oridion Medical recalls Capnostream20 monitors (part CS08750) due to potential resetting of alarm settings when powered off. Affected units may require reconfiguration to prevent safety risks.
The date/time, nurse call and alarm settings of the bedside patient monitors may reset to the factory default settings when the monitor is powered off.
Oridion Medical is recalling Capnostream20 patient monitors that may reset alarm and nurse call settings when powered off. This could lead to missed alarms or incorrect patient monitoring if not properly configured after power cycles.
When the monitor is powered off, the date/time, nurse call, and alarm settings can reset to factory defaults. This may cause alarms to malfunction or patient monitoring to become inaccurate if not manually adjusted after power cycles.
Healthcare professionals using Capnostream20 monitors for patient monitoring are most at risk. Patients in critical care settings may be affected if alarms are reset incorrectly.
Check for the part number CS08750 on the monitor. The product was sold in the US with the model name Capnostream20 (US) M TO MASIMO.
After powering off the monitor, verify that date/time, nurse call, and alarm settings have not reset to factory defaults.
The monitor may reset alarm and nurse call settings to factory defaults when powered off, potentially causing missed alarms or incorrect patient monitoring.
Check for the part number CS08750 on the monitor. The product was sold in the US with the model name Capnostream20 (US) M TO MASIMO.
The recall does not provide a fix; users must manually verify settings after powering off to prevent resets.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0030-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0030-2019 from Oridion Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
